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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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1308907 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
- L7 t2 e$ _5 \/ a; w- U( MNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 : S3 ^9 o, T- b1 n  ?  Y( ^. G  K1 ]
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
3 E% A9 i. ?9 A; M7 L" Z* i- v2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, @8 k; G! r6 u# }+ c6 F3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
1 h" C; Y5 c/ z% G/ n4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
+ q% Z/ b& }; x, V5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 6 Z* X! F" N% c' v* b
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
+ G; a, ^3 M- _: `! n4 K2 h' e7Kinki University School of Medicine, Osaka 589-8511, Japan 2 o# c' @/ V! Z# b1 _4 U. f$ H
8Izumi Municipal Hospital, Osaka 594-0071, Japan
$ Z1 L$ f1 [, t# V2 V+ a; [9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan , x, J. P1 n1 d* z- U
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 ( ~* C6 ?0 Y4 H7 }6 ~
AbstractBackground: 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.
$ B" [$ d. w( l9 h) y' f6 N& f7 H: e* _1 l
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 $ z: E/ e8 P0 j( q" L

2 \& ~; E- y/ k* AAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
+ g+ s. I, f& ~; a6 |6 O+ r3 s0 E" _; |6 b/ E) w
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
8 C; u/ v+ o" j5 P. u( u2 B& k& M0 |/ i3 c( L) A
Published online on: Thursday, December 1, 2011 ! U! P+ s$ `2 y3 l) H+ t

" H5 \7 A- r0 g: RDoi: 10.3892/ol.2011.507
" w2 a! k7 [( h% P4 V: h% k4 z  ?
Pages: 405-410
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Abstract:
* r1 L( u3 e6 b2 t/ ZS-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.9 t0 ]4 Z# X( r8 U7 O" y7 G% D
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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, W7 p) R4 @3 o+ d! a0 N  |- u0 y
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
" Y- T1 J  D5 k- t+ Author Affiliations
/ h3 x, Q! ]& a/ o1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 8 P/ _4 w7 R- S0 [) ~% s) o- F- Y
2Department of Thoracic Surgery, Kyoto University, Kyoto " |$ L6 }2 H2 p1 `
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
( }) O! b  u* U* p* A6 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 ( J* }% O. r# C) j
Received September 3, 2010. # h" N* C" u8 H' L/ m" V
Revision received November 11, 2010.
6 S- T! m  B: q% L: ?9 M9 @Accepted November 17, 2010.
% A5 k/ g! g2 `7 h  M* dAbstract/ h8 @6 P! W" `+ A" H/ j+ [4 n/ ~2 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. 2 n: t1 \" c$ n8 {
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.
6 D0 \/ Q+ Q( W, [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. 3 X  O/ ]3 S: X' i( [, ^. K" j
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ) M$ X. P3 u, R
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。# v- Z' s1 I" ]
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?0 @% d/ h5 O* T" @) `
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
( g9 y/ ~6 b3 x: b8 g  Z. p7 ]& i( {http://clinicaltrials.gov/ct2/show/NCT015235879 D4 h  y7 U6 `) y% D
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
9 i2 y0 x5 o' a: b3 L  zhttp://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
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& l( N" L$ W. t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。
( x% r1 O' _3 R! Y$ Z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
& F/ U5 Q# k/ g5 M& m" f( |- h9 Y* N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。4 S1 `& Z0 g3 J. f! f
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。
% ^# ]( F/ b+ ?" G不错。

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