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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1207374 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
) x$ X' g- B. \$ y5 q; Y) lNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ; G, R# I6 l0 A" Y4 R0 j+ b
+ Author Affiliations8 V+ d# Z# D$ |# {6 m* G
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan " z( Q8 K; r; S7 _' P3 U- l" I& u2 `# x
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 z) u% ?; H7 z" n2 i( E3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 F( ?& W2 X2 F1 {7 _6 i' b2 ^, d4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
" F/ f3 h% z4 n: E/ k5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
; o/ ?9 w" Z9 H: g; r0 b6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ( h# x. C! p7 `# r/ |9 p% v
7Kinki University School of Medicine, Osaka 589-8511, Japan
1 ~( x6 }% G4 l, X& ]4 H- D) t7 G8Izumi Municipal Hospital, Osaka 594-0071, Japan / _, m" v1 J( V- u4 i0 k4 O
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan & `9 Q$ |$ G1 U( ~$ C- P3 J' x
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
" U5 _9 Q2 Y, Y9 o/ CAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. + a' M- s) ]1 Z( b% e

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
+ E: {# ~1 F4 Y6 A( D. x( @3 m
7 D, B7 R% n8 o3 Q. w$ RAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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' f$ q/ f% o! t( a2 f9 Z6 QAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
# p" G' N" B" `- z: L, R% P8 b6 w. F( J; J  a; O
Published online on: Thursday, December 1, 2011
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# m+ T3 v; z+ M$ k: w/ u. H5 i4 UDoi: 10.3892/ol.2011.507 ) q) \/ Q. j* m$ ]. v! {7 L5 J/ t
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Pages: 405-410 ' v  |) I2 L# d" n( F. K

# r4 {# X, w4 }1 p, HAbstract:
" [3 r9 L7 o9 ~8 IS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.0 W- W" R- h" p) B: B5 a. z! K% _

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
% t- w8 I7 V$ X% ^9 iF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
- K  p2 P: K! T/ @6 G/ X- N: \% _+ Author Affiliations
0 t% ~; l/ ?. Z6 O6 Q! i  d, |1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 0 ]7 b/ q2 K) {+ z; U' a0 x
2Department of Thoracic Surgery, Kyoto University, Kyoto
; G; f- a7 r/ E8 K, n, K1 e3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
. ^) z. V* D" x8 t3 }7 p3 z' V&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
$ I* ?2 S% \5 [: E% w) h: v# R! G5 G0 gReceived September 3, 2010.
* Q& _9 [/ K1 }, H1 C* o$ O3 G5 VRevision received November 11, 2010.
7 V$ h/ K+ {  P( F# S7 b, H/ kAccepted November 17, 2010.
6 M& V: s2 q9 O' ]+ U; v  j3 F( bAbstract! n0 Z, [5 N5 L4 S* `$ q6 W7 R
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. 4 @1 C/ H# B- _  h
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. ( p3 H, i$ n/ H9 E( H; _% ?
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. ) s9 y) L6 B6 }- {
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
+ w, L4 C. e. E) v) Q0 ?( w今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?# d: v: \& c! J  o
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
% k' i+ ]# U3 W( f  U* Jhttp://clinicaltrials.gov/ct2/show/NCT01523587' w6 \$ c/ \4 X# w* O' C
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC' x( z" \! G! K$ c) p! Q, B3 t. Q
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 : C  ^/ q9 i6 L" z# q& q7 Z; M
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
9 b' P2 h/ u, f至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53   v! a6 K0 k; [" o7 n: ^. N2 A9 z/ k
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。# `& A; `7 c% @1 x7 M6 |
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
# I( s0 ?9 |7 E9 H5 S不错。

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